US11833367B2ActiveUtilityPatentIndex 62
Methods, devices, and compositions for measuring and inducing cell-to-cell communication, and therapeutic uses thereof
Est. expiryOct 12, 2038(~12.3 yrs left)· nominal 20-yr term from priority
A61N 2005/0661A61N 2005/0659A61M 2037/0007A61N 2/02A61N 5/025A61N 5/062A61K 49/0015A61K 41/0057A61N 5/10A61N 1/403A61M 37/00A61N 5/0622
62
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Cited by
29
References
42
Claims
Abstract
Methods of treating a subject are provided, involving providing a first region of biological material coupled to the subject; initiating a change in a cellular environment of the cells in the first region; and due to a change in biological or chemical activity of the cells in the first region, inducing a biological change in a second region inside the subject, along with various biophoton collectors and biophoton bypasses useful for implementing a variety of the method embodiments.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A method of triggering cell-to-cell communication in a subject comprising:
providing a first region of biological material coupled to the subject;
initiating a change in a cellular environment of the cells in the first region, wherein initiating a change comprises changing a rate of transport of reagents through cell membranes of cells in the biological material of the first region by changing a probability of tunneling of the reagents through cell membranes, wherein changing a probability of tunneling comprises applying a photon flux to the reagents to increase an energy of the reagents; and
due to a change in biological or chemical activity of the cells in the first region, inducing a biological change in a second region inside the subject.
2. The method of claim 1 , further comprising defining for the first region a region inside the subject proximate the second region.
3. The method of claim 2 , wherein the region inside the subject is formed of the subject's own tissue.
4. The method of claim 2 , wherein the region inside the subject is biological material implanted inside the subject.
5. The method of claim 1 , further comprising defining for the first region a region inside the subject remote from the second region.
6. The method of claim 5 , wherein the region inside the subject is formed of the subject's own tissue.
7. The method of claim 5 , wherein the region inside the subject is biological material implanted inside the subject.
8. The method of claim 1 , further comprising defining for the first region a region inside the subject overlapping the second region.
9. The method of claim 1 , wherein providing comprises segregating the biological material of the first region from the second region by an artificial material.
10. The method of claim 9 , wherein the artificial material comprises a material capable of transmission of biophotons therethrough.
11. The method of claim 1 , wherein the first region and the second region are quantum entangled regions.
12. A method of triggering cell-to-cell communication in a subject comprising:
providing a first region of biological material coupled to the subject;
initiating a change in a cellular environment of the cells in the first region; and
due to a change in biological or chemical activity of the cells in the first region, inducing a biological change in a second region inside the subject by coupling to the second region via interactions of DNA molecules along a pathway from the first region to the second region, where coupling comprises having the pathway comprise signaling DNA.
13. A method of triggering cell-to-cell communication in a subject comprising:
providing a first region of biological material coupled to the subject;
initiating a change in a cellular environment of the cells in the first region; and
due to a change in biological or chemical activity of the cells in the first region, inducing a biological change in a second region inside the subject by coupling to the second region via interactions of DNA molecules along a pathway from the first region to the second region, where coupling comprises having the pathway comprise signaling DNA and transporting charge along the signaling DNA.
14. The method of claim 1 , wherein the biological change is a change in viability and wherein the change in the viability of the cells in the first region produces a similar change in the second region of the subject.
15. The method of claim 1 , wherein the biological change in the second region comprises a change in neuron activity.
16. The method of claim 15 , wherein the change in neuron activity is stimulation and/or control of neural communication.
17. The method of claim 12 , further comprising defining for the first region a region inside the subject proximate the second region.
18. The method of claim 17 , wherein the region inside the subject is formed of the subject's own tissue.
19. The method of claim 17 , wherein the region inside the subject is biological material implanted inside the subject.
20. The method of claim 12 , further comprising defining for the first region a region inside the subject remote from the second region.
21. The method of claim 20 , wherein the region inside the subject is formed of the subject's own tissue.
22. The method of claim 20 , wherein the region inside the subject is biological material implanted inside the subject.
23. The method of claim 12 , further comprising defining for the first region a region inside the subject overlapping the second region.
24. The method of claim 12 , wherein providing comprises segregating the biological material of the first region from the second region by an artificial material.
25. The method of claim 24 , wherein the artificial material comprises a material capable of transmission of biophotons therethrough.
26. The method of claim 12 , wherein the first region and the second region are quantum entangled regions.
27. The method of claim 12 , wherein the biological change is a change in viability and wherein the change in the viability of the cells in the first region produces a similar change in the second region of the subject.
28. The method of claim 12 , wherein the biological change in the second region comprises a change in neuron activity.
29. The method of claim 28 , wherein the change in neuron activity is stimulation and/or control of neural communication.
30. The method of claim 13 , further comprising defining for the first region a region inside the subject proximate the second region.
31. The method of claim 30 , wherein the region inside the subject is formed of the subject's own tissue.
32. The method of claim 30 , wherein the region inside the subject is biological material implanted inside the subject.
33. The method of claim 13 , further comprising defining for the first region a region inside the subject remote from the second region.
34. The method of claim 33 , wherein the region inside the subject is formed of the subject's own tissue.
35. The method of claim 33 , wherein the region inside the subject is biological material implanted inside the subject.
36. The method of claim 13 , further comprising defining for the first region a region inside the subject overlapping the second region.
37. The method of claim 13 , wherein providing comprises segregating the biological material of the first region from the second region by an artificial material.
38. The method of claim 37 , wherein the artificial material comprises a material capable of transmission of biophotons therethrough.
39. The method of claim 13 , wherein the first region and the second region are quantum entangled regions.
40. The method of claim 13 , wherein the biological change is a change in viability and wherein the change in the viability of the cells in the first region produces a similar change in the second region of the subject.
41. The method of claim 13 , wherein the biological change in the second region comprises a change in neuron activity.
42. The method of claim 41 , wherein the change in neuron activity is stimulation and/or control of neural communication.Cited by (0)
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